Lescure F, Gurny R, Doelker E
Laboratoires UPSA, Rueil Malmaison, France.
J Biomater Sci Polym Ed. 1995;6(9):797-807. doi: 10.1163/156856295x00184.
New biodegradable polypeptidic copolymers of glutamic acid and tert-butyloxycarbonylmethyl glutamate were evaluated as implantable drug delivery systems. Three copolymers varying in degrees of esterification, which is inversely proportional to the number of glutamic residues, were selected for their range of hydrophilicity and biodegradation rates. Progesterone-containing implants were then prepared by means of an extrusion process and both in vitro and in vivo evaluations were performed. The effects of drug loading, nature, and pH of release medium were investigated. In vitro/in vivo correlations were established for some types of implants. Finally, mathematical fitting of the data, using published models, helped to better understand the mechanisms governing release.
对谷氨酸和叔丁氧羰基甲基谷氨酸的新型可生物降解多肽共聚物作为可植入药物递送系统进行了评估。选择了三种酯化程度不同的共聚物,其与谷氨酸残基数量成反比,因其具有不同的亲水性和生物降解速率范围。然后通过挤压工艺制备含孕酮的植入物,并进行了体外和体内评估。研究了药物负载量、性质和释放介质pH值的影响。为某些类型的植入物建立了体外/体内相关性。最后,使用已发表的模型对数据进行数学拟合,有助于更好地理解释放的控制机制。